Stefan Matile

23.9k total citations · 5 hit papers
392 papers, 20.1k citations indexed

About

Stefan Matile is a scholar working on Molecular Biology, Organic Chemistry and Materials Chemistry. According to data from OpenAlex, Stefan Matile has authored 392 papers receiving a total of 20.1k indexed citations (citations by other indexed papers that have themselves been cited), including 199 papers in Molecular Biology, 131 papers in Organic Chemistry and 114 papers in Materials Chemistry. Recurrent topics in Stefan Matile's work include Molecular Sensors and Ion Detection (93 papers), Lipid Membrane Structure and Behavior (82 papers) and Supramolecular Self-Assembly in Materials (66 papers). Stefan Matile is often cited by papers focused on Molecular Sensors and Ion Detection (93 papers), Lipid Membrane Structure and Behavior (82 papers) and Supramolecular Self-Assembly in Materials (66 papers). Stefan Matile collaborates with scholars based in Switzerland, United States and Spain. Stefan Matile's co-authors include Naomi Sakai, Jiri Mareda, Eric Vauthey, Giulio Gasparini, Andreas Vargas Jentzsch, Sebastian Benz, Aurélien Roux, Javier López‐Andarias, Javier Montenegro and Eun‐Kyoung Bang and has published in prestigious journals such as Science, Chemical Reviews and Proceedings of the National Academy of Sciences.

In The Last Decade

Stefan Matile

387 papers receiving 20.0k citations

Hit Papers

Role of LBPA and Alix in ... 2004 2026 2011 2018 2004 2010 2010 2018 2018 100 200 300 400 500

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Stefan Matile 8.3k 7.3k 5.9k 5.1k 3.2k 392 20.1k
Naomi Sakai 5.7k 0.7× 5.2k 0.7× 4.2k 0.7× 3.2k 0.6× 2.3k 0.7× 286 14.1k
Andrew D. Hamilton 17.3k 2.1× 10.0k 1.4× 5.0k 0.8× 4.6k 0.9× 1.8k 0.6× 447 30.1k
Christopher A. Hunter 6.2k 0.8× 10.9k 1.5× 8.7k 1.5× 5.4k 1.1× 7.1k 2.2× 316 23.6k
Yoshihisa Inoue 4.4k 0.5× 11.8k 1.6× 8.1k 1.4× 7.3k 1.4× 2.9k 0.9× 528 21.4k
Françisco M. Raymo 3.2k 0.4× 9.0k 1.2× 11.5k 1.9× 5.4k 1.1× 2.0k 0.6× 257 19.8k
Eric V. Anslyn 8.7k 1.1× 7.9k 1.1× 8.8k 1.5× 13.9k 2.7× 1.3k 0.4× 421 25.5k
Christoph A. Schalley 2.6k 0.3× 8.4k 1.1× 4.5k 0.8× 5.6k 1.1× 2.3k 0.7× 305 14.0k
Santanu Bhattacharya 7.0k 0.8× 5.5k 0.8× 5.2k 0.9× 2.8k 0.5× 858 0.3× 389 15.9k
Steven C. Zimmerman 4.7k 0.6× 6.4k 0.9× 3.7k 0.6× 1.9k 0.4× 1.3k 0.4× 220 13.5k
Werner M. Nau 3.5k 0.4× 12.1k 1.6× 6.7k 1.1× 9.2k 1.8× 5.8k 1.8× 332 19.2k

Countries citing papers authored by Stefan Matile

Since Specialization
Citations

This map shows the geographic impact of Stefan Matile's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Stefan Matile with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stefan Matile more than expected).

Fields of papers citing papers by Stefan Matile

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stefan Matile. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Stefan Matile. The network helps show where Stefan Matile may publish in the future.

Co-authorship network of co-authors of Stefan Matile

This figure shows the co-authorship network connecting the top 25 collaborators of Stefan Matile. A scholar is included among the top collaborators of Stefan Matile based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Stefan Matile. Stefan Matile is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Sakai, Naomi, et al.. (2025). Thiol-mediated uptake of phosphorothioate liposomes, visualized with fluorescent flippers. Chemical Science. 16(40). 18599–18606.
2.
Chen, Dongping, Rosa M. Gomila, Antonio Frontera, et al.. (2024). Pnictogen‐Bonding Enzymes. Angewandte Chemie International Edition. 63(45). e202411347–e202411347. 17 indexed citations
3.
Thorn‐Seshold, Oliver, et al.. (2024). Selenium‐Centered Cascade Exchangers and Conformational Control Unlock Unique Patterns of Thiol‐Mediated Cellular Uptake. SHILAP Revista de lepidopterología. 2(5). 8 indexed citations
4.
Maillard, Jimmy, Karolína Straková, José García‐Calvo, et al.. (2024). Single-Molecule Localization Microscopy and Tracking with a Fluorescent Mechanosensitive Probe. The Journal of Physical Chemistry B. 128(33). 7997–8006. 1 indexed citations
5.
Chen, Xiaoxiao, et al.. (2023). Hydrophobic Interfacing of Fluorescent Membrane Probes. SHILAP Revista de lepidopterología. 1(3). 6 indexed citations
7.
Kato, Takehiro, Bumhee Lim, Yangyang Cheng, et al.. (2022). Cyclic Thiosulfonates for Thiol-Mediated Uptake: Cascade Exchangers, Transporters, Inhibitors. JACS Au. 2(4). 839–852. 20 indexed citations
9.
Menin, Laure, Natalia Gasilova, Sebastian Götze, et al.. (2022). Tyrosine bioconjugation with hypervalent iodine. Chemical Science. 13(43). 12808–12817. 25 indexed citations
10.
Lim, Bumhee, Yangyang Cheng, Takehiro Kato, et al.. (2021). Inhibition of Thiol‐Mediated Uptake with Irreversible Covalent Inhibitors. Helvetica Chimica Acta. 104(8). 21 indexed citations
11.
Colom, Adai, Stefan Matile, Frédérique Pompeo, et al.. (2020). High-speed atomic force microscopy highlights new molecular mechanism of daptomycin action. Nature Communications. 11(1). 6312–6312. 49 indexed citations
12.
Cheng, Yangyang, Anh‐Tuan Pham, Takehiro Kato, et al.. (2020). Inhibitors of thiol-mediated uptake. Chemical Science. 12(2). 626–631. 52 indexed citations
13.
Gini, Andrea, Miguel Paraja, Bartomeu Galmés, et al.. (2020). Pnictogen-bonding catalysis: brevetoxin-type polyether cyclizations. Chemical Science. 11(27). 7086–7091. 81 indexed citations
14.
Jiménez‐Rojo, Noemi, Manuel D. Leonetti, Valeria Zoni, et al.. (2020). Conserved Functions of Ether Lipids and Sphingolipids in the Early Secretory Pathway. Current Biology. 30(19). 3775–3787.e7. 45 indexed citations
15.
Riggi, Margot, Clélia Bourgoint, Mariano Macchione, et al.. (2019). TORC2 controls endocytosis through plasma membrane tension. The Journal of Cell Biology. 218(7). 2265–2276. 42 indexed citations
16.
Okamoto, Yasunori, Ryosuke Kojima, Fabian Schwizer, et al.. (2018). A cell-penetrating artificial metalloenzyme regulates a gene switch in a designer mammalian cell. Nature Communications. 9(1). 1943–1943. 105 indexed citations
17.
Bauzá, Antonio, Alexander Aster, Marion Pupier, et al.. (2018). Synergistic Anion–(π)n–π Catalysis on π-Stacked Foldamers. Journal of the American Chemical Society. 140(14). 4884–4892. 89 indexed citations
18.
Riggi, Margot, Nicolas Chiaruttini, Adai Colom, et al.. (2018). Decrease in plasma membrane tension triggers PtdIns(4,5)P2 phase separation to inactivate TORC2. Nature Cell Biology. 20(9). 1043–1051. 107 indexed citations
19.
Benz, Sebastian, Javier López‐Andarias, Jiri Mareda, Naomi Sakai, & Stefan Matile. (2016). Catalysis with Chalcogen Bonds. Angewandte Chemie. 129(3). 830–833. 85 indexed citations
20.
Matsuo, Hirotami, Julien Chevallier, Nathalie Mayran, et al.. (2004). Role of LBPA and Alix in Multivesicular Liposome Formation and Endosome Organization. Science. 303(5657). 531–534. 563 indexed citations breakdown →

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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